USD 84.99 The presence and extension of late gadolinium enhancement (LGE) are independent predictors of ventricular arrhythmia, systolic dysfunction, all-cause mortality, and sudden cardiac death.
Neben Nonischemic Kardiomyopathie hat NICM andere Bedeutungen. Papers These abnormal heart rhythms can result in fainting or, in some cases, sudden death if your heart stops beating effectively. Nonischemic cardiomyopathy comprises a heterogenous group of myocardial disorders that are not caused by hemodynamic disturbances such as hypertension, valve disease, obstructive coronary artery disease, or congenital heart disease and involves structural and/or functional myocardial abnormalities. Cardiomyopathy (kahr-dee-o-my-OP-uh-thee) is a disease of the heart muscle that makes it harder for your heart to pump blood to the rest of your body. Any use of this site constitutes your agreement to the Terms and Conditions and Privacy Policy linked below. Most affected people have a family history of the disease, and some genetic mutations have been linked to hypertrophic cardiomyopathy.Restrictive cardiomyopathy can occur for no known reason (idiopathic), or it can by caused by a disease elsewhere in the body that affects the heart, such as when iron builds up in the heart muscle (hemochromatosis).There are a number of factors that can increase your risk of cardiomyopathy, including:As your heart weakens, such as in heart failure, it begins to enlarge, forcing your heart to work harder to pump blood to the rest of your body.Cardiomyopathy can lead to other heart conditions, including:In many cases, you can't prevent cardiomyopathy. INTRODUCTION. The most common cause is coronary artery disease or heart attack.Hypertrophic cardiomyopathy can develop at any age, but the condition tends to be more severe if it becomes apparent during childhood. The hallmarks of DCM are left or often biventricular enlargement with mostly global systolic hypokinesis, although some regionally more pronounced contraction abnormality may be present.
In some people, however, it's the result of another condition (acquired) or passed on from a parent (inherited).Contributing factors for acquired cardiomyopathy include:Compared with a normal heart, dilated cardiomyopathy causes the chambers of the heart to enlarge, which can lead to heart failure if left untreated.Illustrations of a normal heart (left) and a heart with hypertrophic cardiomyopathy.
In many cases, you can't prevent cardiomyopathy. EndNote Call 911 or your local emergency number if you have severe difficulty breathing, fainting or chest pain that lasts for more than a few minutes.Because some types of cardiomyopathy can be hereditary, if you have it your doctor might advise that your family members be checked.Often the cause of the cardiomyopathy is unknown. A rigorous work-up can exclude alternative causes of left ventricular (LV) dilation and dysfunction, identify etiologies that may respond to specific treatments, and guide family screening.
Zotero This service is more advanced with JavaScript availableNonischemic cardiomyopathy comprises a heterogenous group of myocardial disorders that are not caused by hemodynamic disturbances such as hypertension, valve disease, obstructive coronary artery disease, or congenital heart disease and involves structural and/or functional myocardial abnormalities.
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Introduction and Classification. Cardiac magnetic resonance (CMR) has an important role in the diagnosis, classification, and risk stratification of patients with suspected or established cardiomyopathies.
In contrast to ischemic cardiomyopathy (ICM), nonischemic cardiomyopathy (NICM) consists of a heterogeneous group of diseases,1 affecting the myocardium without the presence of any significant coronary artery disease. Reference Manager
Papers © 1998-2020 Mayo Foundation for Medical Education and Research (MFMER).
Objectives The study sought to examine prognostic relevance of T1 mapping parameters (based on a T1 mapping method) in nonischemic dilated cardiomyopathy (NIDCM) and compare them with conventional markers of adverse outcome.
RefWorks "Mayo," "Mayo Clinic," "MayoClinic.org," "Mayo Clinic Healthy Living," and the triple-shield Mayo Clinic logo are trademarks of Mayo Foundation for Medical Education and Research. Note that the heart walls (muscles) are much thicker (hypertrophied) in the heart with hypertrophic cardiomyopathy.Although this type can affect people of all ages, it occurs most often in middle-aged people and is more likely to affect men.
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